At Vedrax SAS, I lead the architecture and development of pharmaceutical software, working with a Senior R&D CMC Manager to turn laboratory, bioequivalence, and regulatory requirements into digital solutions. I designed and developed a bespoke LIMS for a pharmaceutical CRO, a RIMS for regulatory information and submission lifecycle management, and an application for in-vitro bioequivalence studies.
At European Dynamics, I work on large-scale European institutional information systems, including architecture and operation of EEA ReportNet3 core microservices and architecture and implementation for EUR-Lex. My work spans solution and integration architecture, Kafka-based asynchronous systems, and compliance intelligence that connects regulatory changes with controls and SOP versions.
